반응 #323040

ord-fb9827c73e1245b394d8bb3d31b4abe0

용매

반응 조건

온도
4°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.DISSOLUTIONis dissolved
  2. 2
    기타the crystallised solid is separated by filtration
  3. 3
    세척washed with ethanol (2×10 cc)
  4. 4
    기타dried at 45° C. under reduced pressure (0.067 kPa)

실험 절차

The procedure is similar to that described in Example 1, but starting with 2-furancarboxylic acid (8.95 g), N,N'-carbonyldiimidazole (12.8 g) and 2-amino-7-methoxy-1,8-naphthyridine (10.5 g). The product produced by precipitation in water (15.5 g; m.p. 199° C.) is dissolved in boiling ethanol (500 cc). After 2 hours' cooling at 4° C., the crystallised solid is separated by filtration, washed with ethanol (2×10 cc) and dried at 45° C. under reduced pressure (0.067 kPa). N-(7-Methoxy-1,8-naphthyridin-2-yl)-2-furancarboxamide (13.5 g) is produced, m.p. 201° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04642308uspto-grants-1987_02